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Overexpression of CCL-20 and CXCL-8 genes enhances tumor escape and resistance to cemiplimab, a programmed cell death protein-1 (PD-1) inhibitor, in patients with locally advanced and metastatic cutaneous squamous cell carcinoma.
- Source :
-
Oncoimmunology [Oncoimmunology] 2024 Aug 26; Vol. 13 (1), pp. 2388315. Date of Electronic Publication: 2024 Aug 26 (Print Publication: 2024). - Publication Year :
- 2024
-
Abstract
- Cemiplimab has demonstrated relevant clinical activity in cutaneous squamous cell carcinoma (cSCC) but mechanisms of primary and acquired resistance to immunotherapy are still unknown. We collected clinical data from locally advanced and/or metastatic cSSC patients treated with cemiplimab in two Italian University centers. In addition, gene expression analysis by using Nanostring Technologies platform to evaluate 770 cancer- and immune-related genes on 20 tumor tissue samples (9 responders and 11 non-responders to cemiplimab) was performed. We enrolled 81 patients with a median age of 82 years. After 16.4 months of median follow-up, 12- and 24-months PFS were 53% and 42%, respectively; while 12- and 24-months OS were 71% and 61%, respectively. Treatment was well tolerated. Overall response rate (ORR) was 58%, with a disease control rate (DCR) of 77.8%. The difference between genes expressed in responder versus non-responder patient samples was substantial, particularly for genes involved in immune system regulation. Cemiplimab-resistant tumors were associated with over-expression of CCL-20 and CXCL-8. Cemiplimab confirmed efficacy and safety data in real-life cSCC patients. Overexpression of CCL-20 and CXCL-8 could represent biomarkers of lack of response to immunotherapy.<br />Competing Interests: S.N. had travel grants from Amgen, Merck outside of the submitted works. D.C. had travel support from Sanofi, BMS, Merck serono outside of the submitted works. F.C. was advisory board for Amgen, Servier, MSD, Merck, Roche, Pfizer, Bayer, Pierre Fabre, Eisai outside of the submitted work. T.T. was advisory board for Amgen, MSD, Pierre Fabre, Roche, Merck outside of the submitted work. All remaining authors have no competing interests.<br /> (© 2024 The Author(s). Published with license by Taylor & Francis Group, LLC.)
- Subjects :
- Humans
Male
Female
Aged
Aged, 80 and over
Tumor Escape drug effects
Tumor Escape genetics
Middle Aged
Immune Checkpoint Inhibitors therapeutic use
Immune Checkpoint Inhibitors pharmacology
Programmed Cell Death 1 Receptor antagonists & inhibitors
Programmed Cell Death 1 Receptor genetics
Programmed Cell Death 1 Receptor metabolism
Gene Expression Regulation, Neoplastic drug effects
Antineoplastic Agents, Immunological therapeutic use
Antineoplastic Agents, Immunological pharmacology
Antibodies, Monoclonal, Humanized therapeutic use
Antibodies, Monoclonal, Humanized pharmacology
Antibodies, Monoclonal, Humanized administration & dosage
Skin Neoplasms drug therapy
Skin Neoplasms genetics
Skin Neoplasms pathology
Carcinoma, Squamous Cell drug therapy
Carcinoma, Squamous Cell genetics
Carcinoma, Squamous Cell pathology
Drug Resistance, Neoplasm genetics
Drug Resistance, Neoplasm drug effects
Interleukin-8 genetics
Interleukin-8 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2162-402X
- Volume :
- 13
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Oncoimmunology
- Publication Type :
- Academic Journal
- Accession number :
- 39206096
- Full Text :
- https://doi.org/10.1080/2162402X.2024.2388315